Associated Papers
Clinical and molecular response of acute myeloid leukemia harboring non-canonical FLT3 N676K driver mutations to contemporary FLT3 inhibitors.
Roloff GW et al.
Haematologica, 2023
36655425 (PubMed )
Supplement: 2022_282148_ROLOFF_SUPPL.pdf
Inflammatory Breast Cancer: Clinical Implications of Genomic Alterations and Mutational Profiling.
Faldoni FLC et al.
Cancers, 2020
33007869 (PubMed )
Supplement: cancers-12-02816-s001.zip › Table_S10.xlsx › Table_S10
Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
Yehia L et al.
Plos Genetics, 2018
29684080 (PubMed )
Supplement: pgen.1007352.s010.xlsx › S9_Table
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Bekheirnia MR et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
27657687 (PubMed )
Supplement: NIHMS807719-supplement-Table_S2_S3.xlsx › Table_S2
Select a paper to view details